We're looking at: The millions of adults with Spastic Cerebral Palsy - 70% of all cases. Schemes for the future including facilities, centres and the various treatments available. The way CP is defined in different cultures, How to improve the support systems, or to create them; how to permanently enable self-advocacy, and raise awareness more generally. With the power of shared information these many millions of adults will stop being left in an informational void; it's about quality of life improvement, and if we act now with your help that difference can be made. The social and medical injustices of information black-holes will be neutralised. That's something not just people with Spastic CP would want and need, but what everyone should want and need. Tight muscles are a specific kind of threat to the individual with Spasticity, but the lack of information that prevents already-existing treatment is the type of threat that speaks to every human on earth.

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